QC SPF 30 Sunscreen

Product NDC
63868-913
11-digit product format
638680913
Labeler code
63868
Product ID
63868-913_2957af4d-11df-3abe-e063-6394a90a2eff
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 6%
Dosage form
LOTION
Route
TOPICAL
Labeler
CDMA
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-12-22
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 15; 5; 6 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
QC SPF 30 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100g
HOMOSALATE15 g/100g
OCTISALATE5 g/100g
OCTOCRYLENE6 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-913-08QC SPF 30 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2272

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-913QC SPF 30 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 6%) LOTION [CDMA]2Current NDC, 1 package rows20241217_f80ceb05-0bd4-1355-e053-6294a90afb19.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
63868-913-0863868091308227 g in 1 BOTTLE, PLASTIC (63868-913-08) 227 g2021-12-22NoNoCurrent